A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156438



Internal ID22086839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:314962..381149hg38UCSC Ensembl
Outerchr6:303121..382559hg38UCSC Ensembl
Innerchr6:314962..381149hg19UCSC Ensembl
Outerchr6:303121..382559hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3879439
hg1979439
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv241n97
Supporting Variantsnssv4018291
Samples
Known GenesDUSP22
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156438
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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